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rs121434386

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121434386(C;T)
Make rs121434386(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position118141265
GeneSCN4B
is asnp
is mentioned by
dbSNPrs121434386
ebirs121434386
HLIrs121434386
Exacrs121434386
Varsomers121434386
Maprs121434386
PheGenIrs121434386
hapmaprs121434386
1000 genomesrs121434386
hgdprs121434386
ensemblrs121434386
gopubmedrs121434386
geneviewrs121434386
scholarrs121434386
googlers121434386
pharmgkbrs121434386
gwascentralrs121434386
openSNPrs121434386
23andMers121434386
23andMe allrs121434386
SNP Nexus

SNPshotrs121434386
SNPdbers121434386
MSV3drs121434386
GWAS Ctlgrs121434386
Max Magnitude0
OMIM608256
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121434386(T;T)
Alt rs121434386(T;T)
Reference rs121434386(C;C)
Significance Pathogenic
Disease Long QT syndrome 10
Variation info
Gene SCN4B
CLNDBN Long QT syndrome 10
Reversed 1
HGVS NC_000011.9:g.118011980G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000002563.2,